- Analytical Method Development (e.g. Assay Related substance and dissolution by Chromatographic methods)
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- Analytical method validation and method transfer.
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- Preparation of specification, standard test procedure, Method development Reports of drug products and excipients.
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- Maintenance and upkeep of the GLP documents.
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- Maintain GLP environment.
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- To provide timely support in resolving regulatory quires.
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- To help and supports site QC investigations
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